TESMIN
Tesmin
Also known as: CXCDC2, MTL5, MTL5_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y4I5
- Gene
- TESMIN
- Ensembl
- ENSG00000132749
- Chromosome
- 11
- Canonical length
- 508 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
OverviewNCBI Gene
Metallothionein proteins are highly conserved low-molecular-weight cysteine-rich proteins that are induced by and bind to heavy metal ions and have no enzymatic activity. They may play a central role in the regulation of cell growth and differentiation and are involved in spermatogenesis. This gene encodes a metallothionein-like protein which has been shown to be expressed differentially in mouse testis and ovary. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
508 residues, UniProt reviewed canonical sequence.
>Q9Y4I5|TESMIN
1 MEEGPLPGGL PSPEDAMVTE LLSPEGPFAS ENIGLKAPVK YEEDEFHVFK EAYLGPADPK
61 EPVLHAFNPA LGADCKGQVK AKLAGGDSDG GELLGEYPGI PELSALEDVA LLQAPQPPAC
121 NVHFLSSLLP AHRSPAVLPL GAWVLEGASH PGVRMIPVEI KEAGGTTTSN NPEEATLQNL
181 LAQESCCKFP SSQELEDASC CSLKKDSNPM VICQLKGGTQ MLCIDNSRTR ELKALHLVPQ
241 YQDQNNYLQS DVPKPMTALV GRFLPASTKL NLITQQLEGA LPSVVNGSAF PSGSTLPGPP
301 KITLAGYCDC FASGDFCNNC NCNNCCNNLH HDIERFKAIK ACLGRNPEAF QPKIGKGQLG
361 NVKPQHNKGC NCRRSGCLKN YCECYEAQIM CSSICKCIGC KNYEESPERK TLMSMPNYMQ
421 TGGLEGSHYL PPTKFSGLPR FSHDRRPSSC ISWEVVEATC ACLLAQGEEA EKEHCSKCLA
481 EQMILEEFGR CLSQILHTEF KSKGLKMELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TESMIN can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.59
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- testis: 49 nTPM
- bone marrow: 7 nTPM
- breast: 4 nTPM
- kidney: 3.2 nTPM
- rectum: 2.8 nTPM
- colon: 2.4 nTPM
Single-cell type
- late primary spermatocytes: 247 nCPM
- late spermatids: 215 nCPM
- early primary spermatocytes: 132 nCPM
- early spermatids: 106 nCPM
- oocytes: 78 nCPM
- endometrial luminal cells: 48 nCPM
Immune cell
- neutrophil: 0.5 nTPM
- classical monocyte: 0.2 nTPM
- eosinophil: 0.2 nTPM
- memory CD4 T-cell: 0.2 nTPM
- non-classical monocyte: 0.2 nTPM
- MAIT T-cell: 0.1 nTPM
Brain region
- pons: 4.1 nTPM
- hypothalamus: 3.3 nTPM
- medulla oblongata: 3.3 nTPM
- basal ganglia: 3 nTPM
- midbrain: 3 nTPM
- cerebellum: 2.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.85
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- intracellular monoatomic cation homeostasis
- male meiotic nuclear division
- regulation of DNA-templated transcription
- response to metal ion
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TESMIN as an antibody target. Whether an autoantibody or antibody against TESMIN could matter depends on whether native TESMIN is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TESMIN is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TESMIN as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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